Person who experienced the adverse event (patient)
| Event ID | CASEID | CASEVERSION | I F COD | EVENT DT | MFR DT | INIT FDA DT | FDA DT | REPT COD | AUTH NUM | MFR NUM | MFR SNDR | LIT REF | AGE | AGE COD | AGE GRP | GNDR COD | E SUB | WT | WT COD | REPT DT | TO MFR | OCCP COD | REPORTER COUNTRY | OCCR COUNTRY |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 88109566 | 8810956 | 6 | F | 2011 | 20160714 | 20120927 | 20160726 | EXP | BR-AMGEN-BRASP2012009138 | AMGEN | 54.00 | YR | A | F | Y | 71.00000 | KG | 20160726 | CN | BR | BR |
Drug(s) used by person
| Event ID | CASEID | DRUG SEQ | ROLE COD | DRUGNAME | PROD AI | VAL VBM | ROUTE | DOSE VBM | CUM DOSE CHR | CUM DOSE UNIT | DECHAL | RECHAL | LOT NUM | EXP DT | NDA NUM | DOSE AMT | DOSE UNIT | DOSE FORM | DOSE FREQ |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 88109566 | 8810956 | 1 | PS | ENBREL | ETANERCEPT | 1 | Unknown | 50 MG, ONCE A WEEK | Y | 103795 | 50 | MG | POWDER AND SOLVENT FOR SOLUTION FOR INJECTION | /wk | |||||
| 88109566 | 8810956 | 2 | SS | ENBREL | ETANERCEPT | 1 | Subcutaneous | 50 MG, WEEKLY | Y | 103795 | 50 | MG | POWDER AND SOLVENT FOR SOLUTION FOR INJECTION | /wk | |||||
| 88109566 | 8810956 | 3 | SS | ENBREL | ETANERCEPT | 1 | Unknown | 50 UNK, QWK | Y | 103795 | POWDER AND SOLVENT FOR SOLUTION FOR INJECTION | /wk | |||||||
| 88109566 | 8810956 | 4 | C | METHOTREXATE. | METHOTREXATE | 1 | UNK | 0 | |||||||||||
| 88109566 | 8810956 | 5 | C | PREDNISONE. | PREDNISONE | 1 | 5 MG, ONCE A DAY | 0 | 5 | MG | QD | ||||||||
| 88109566 | 8810956 | 6 | C | PREDNISONE. | PREDNISONE | 1 | 0 | ||||||||||||
| 88109566 | 8810956 | 7 | C | CALCIUM D /01272001/ | 2 | UNK | 0 | ||||||||||||
| 88109566 | 8810956 | 8 | C | IBUPROFEN. | IBUPROFEN | 1 | UNK, AS NEEDED | 0 | |||||||||||
| 88109566 | 8810956 | 9 | C | FOLIC ACID. | FOLIC ACID | 1 | 5 MG, ONCE A WEEK | 0 | 5 | MG | /wk | ||||||||
| 88109566 | 8810956 | 10 | C | CALCIUM | CALCIUM | 1 | 600 MG, 2X/DAY | 0 | 600 | MG | BID |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 88109566 | 8810956 | 1 | Rheumatoid arthritis |
| 88109566 | 8810956 | 5 | Arthritis |
| 88109566 | 8810956 | 6 | Rheumatoid arthritis |
| 88109566 | 8810956 | 7 | Osteoporosis |
| 88109566 | 8810956 | 8 | Pain |
| 88109566 | 8810956 | 9 | Rheumatoid arthritis |
| 88109566 | 8810956 | 10 | Osteoporosis |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 88109566 | 8810956 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 88109566 | 8810956 | Alopecia | |
| 88109566 | 8810956 | Arthropathy | |
| 88109566 | 8810956 | Condition aggravated | |
| 88109566 | 8810956 | Injection site pain |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| Event ID | CASEID | DSG DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|---|
| 88109566 | 8810956 | 1 | 20110105 | 0 | ||
| 88109566 | 8810956 | 2 | 201103 | 201111 | 0 | |
| 88109566 | 8810956 | 3 | 2015 | 0 |